Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs13072552
rs13072552
CP
2 1.000 0.080 3 149195339 intron variant G/T snv 0.18 0.800 1.000 1 2012 2012